OBO ID: DOID:0060213
Term Name: frontotemporal dementia and/or amyotrophic lateral sclerosis 1 Search Ontology:
Synonyms:
  • ALSFTD
  • amyotrophic lateral sclerosis and/or frontotemporal dementia
  • frontotemporal dementia and/or motor neuron disease
  • FTDALS1
  • FTDMND
Definition: An amyotrophic lateral sclerosis that has_material_basis_in mutation in the C9ORF72 gene on chromosome 9. It is characterized by adult onset of either frontotemporal dementia and/or amyotrophic lateral sclerosis. http://omim.org/entry/105550
References:
Ontology: Human Disease   ( DOID:0060213 )
Relationships
is a type of:
OTHER frontotemporal dementia and/or amyotrophic lateral sclerosis 1 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
C9orf72 Frontotemporal dementia and/or amyotrophic lateral sclerosis 1 105550
PHENOTYPE No data available

CITATIONS (1)
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